TY - JOUR
T1 - Unanticipated Cardiotoxicity Associated with Targeted Anticancer Therapy in Patients with Hematologic Malignancies Patients
T2 - Natural History and Risk Factors
AU - Shah, Chintan
AU - Gong, Yan
AU - Szady, Anita
AU - Sun, Qian
AU - Pepine, Carl J.
AU - Langaee, Taimour
AU - Lucas, Alexandra R.
AU - Moreb, Jan S.
N1 - Funding Information:
Acknowledgements Dr. Pepine receives support from the NIH-NHLBI-5 UM1 HL087366-10; 1R01HL132448-01; 5 R01 HL033610-29; 5 R01 HL056921-19; and NCATS-University of Florida Clinical and Translational Science UL1TR001427; PCORnet—OneFlorida Clinical Research Consortium CDRN-1501-26692 and the Gatorade Trust through funds distributed by the University of Florida, Department of Medicine.
Publisher Copyright:
© 2017, Springer Science+Business Media, LLC.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Our aim is to study unanticipated cardiotoxicity associated with the use of anticancer targeted agents, a problem that remains poorly understood. Using diagnosis codes, we retrospectively identified patients with both hematologic malignancies (HM) and cardiovascular diseases (n = 820 patients). Cardiotoxicity was defined per published criteria. The targeted agents of interest included tyrosine kinase inhibitors, proteasome inhibitors, monoclonal antibodies, and immunomodulatory agents. Patients found with cardiotoxicity (n = 29) were compared with 70 case-matched reference subjects. Median time from targeted therapy exposure to cardiotoxicity was 132 days. A higher percentage of patients had prior exposure to anthracyclines in study versus reference group (65.5 vs. 42.8%, P = 0.04), however, did not stay significant in multivariate analysis. Two variables were significant predictors, prior of DVT/PE and Karnofsky score of ≥ 80% (P ≤ 0.011). Only 2 study group patients died of cardiac causes. Most cardiotoxicity patients (23/29) had remained stable or improved, while 21 patients received further chemotherapy. OS was lower in the study group (P = 0.018) versus the reference group. In conclusion, a small number patients with HM experience unanticipated cardiotoxicity with low related mortality. Risk of cardiotoxicity was significantly associated with history of DVT/PE. Most patients do well, but despite that, their OS is significantly poorer.
AB - Our aim is to study unanticipated cardiotoxicity associated with the use of anticancer targeted agents, a problem that remains poorly understood. Using diagnosis codes, we retrospectively identified patients with both hematologic malignancies (HM) and cardiovascular diseases (n = 820 patients). Cardiotoxicity was defined per published criteria. The targeted agents of interest included tyrosine kinase inhibitors, proteasome inhibitors, monoclonal antibodies, and immunomodulatory agents. Patients found with cardiotoxicity (n = 29) were compared with 70 case-matched reference subjects. Median time from targeted therapy exposure to cardiotoxicity was 132 days. A higher percentage of patients had prior exposure to anthracyclines in study versus reference group (65.5 vs. 42.8%, P = 0.04), however, did not stay significant in multivariate analysis. Two variables were significant predictors, prior of DVT/PE and Karnofsky score of ≥ 80% (P ≤ 0.011). Only 2 study group patients died of cardiac causes. Most cardiotoxicity patients (23/29) had remained stable or improved, while 21 patients received further chemotherapy. OS was lower in the study group (P = 0.018) versus the reference group. In conclusion, a small number patients with HM experience unanticipated cardiotoxicity with low related mortality. Risk of cardiotoxicity was significantly associated with history of DVT/PE. Most patients do well, but despite that, their OS is significantly poorer.
KW - Cardiotoxicity
KW - Hematologic malignancies
KW - Targeted therapy
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U2 - 10.1007/s12012-017-9429-8
DO - 10.1007/s12012-017-9429-8
M3 - Article
C2 - 29022233
AN - SCOPUS:85031103933
SN - 1530-7905
VL - 18
SP - 184
EP - 191
JO - Cardiovascular Toxicology
JF - Cardiovascular Toxicology
IS - 2
ER -